首页> 外文会议>Joint RECOMB 2006 Satellite Workshops on Systems Biology and on Computational Proteomics; 20061201-03; San Diego,CA(US) >A Context-Specific Network of Protein-DNA and Protein-Protein Interactions Reveals New Regulatory Motifs in Human B Cells
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A Context-Specific Network of Protein-DNA and Protein-Protein Interactions Reveals New Regulatory Motifs in Human B Cells

机译:特定于上下文的蛋白质-DNA和蛋白质-蛋白质相互作用网络揭示了人类B细胞中的新调控基元。

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Recent genome wide studies in yeast have started to unravel the complex, combinatorial nature of transcriptional regulation in eukaryotic cells, including the concerted regulation of proteins involved in complex formation. In this work, we use a Bayesian evidence integration framework to assemble an integrated network, including both protein-DNA and protein-protein interactions, in a specific cellular con-text(human B cells). We then use it to study common interaction motifs between protein complexes and regulatory programs, using an enrichment analysis approach. Specifically, we compare the frequency of mixed interaction motifs in the real network against random networks of equivalent connectivity. These motifs include sets of target genes regulated by multiple interacting transcription-factors, and gene sets encoding same complex proteins regulated by different transcription factors.
机译:最近在酵母中进行的全基因组研究已开始揭示真核细胞转录调控的复杂,组合性质,包括参与复合物形成的蛋白质的协调调控。在这项工作中,我们使用贝叶斯证据集成框架在特定的细胞环境(人B细胞)中组装一个包括蛋白质-DNA和蛋白质-蛋白质相互作用的整合网络。然后,我们使用一种富集分析方法,使用它来研究蛋白质复合物和调控程序之间的常见相互作用基序。具体来说,我们比较了实际网络中混合互动主题的频率与等效连接性的随机网络的频率。这些基序包括受多种相互作用转录因子调节的靶基因组,以及编码受不同转录因子调节的相同复杂蛋白的基因组。

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